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特发性内源性类脂性肺炎

Idiopathic endogenous lipoid pneumonia.

作者信息

Sharma Aman, Ohri Shivani, Bambery Pradeep, Singh Surjit

机构信息

Department of Internal Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Indian J Chest Dis Allied Sci. 2006 Apr-Jun;48(2):143-5.

Abstract

Lipoid pneumonia is a rare pulmonary disorder having no classical radiological appearance. We report a 33-year-old male, ex-smoker who was referred to us with history of cough, mild mucoid expectoration and progressively increasing dyspnoea since one year. He was investigated at local hospital and was treated with 30 mg prednisolone per day for 6 months for sarcoidosis without any response. On examination, he was normal except for fine basal crepitations in chest. Pulmonary function test (PFT) revealed mild airway obstruction. High resolution computerised tomographic scan (HRCT scan) revealed bilateral reticulonodular shadows and bronchiectasis in lower zones. Open lung biopsy revealed lipoid pneumonia. As there was no history of nasal distillation of oils, it was diagnosed to be idiopathic. The relevant literature is reviewed.

摘要

类脂性肺炎是一种罕见的肺部疾病,没有典型的放射学表现。我们报告一名33岁男性,既往吸烟,因咳嗽、轻度黏液样咳痰及渐进性加重的呼吸困难1年前来就诊。他在当地医院接受了检查,并因结节病接受了每天30毫克泼尼松龙治疗6个月,但无任何反应。检查时,除胸部底部有细微捻发音外,他身体正常。肺功能测试(PFT)显示轻度气道阻塞。高分辨率计算机断层扫描(HRCT扫描)显示双肺下叶网状结节影及支气管扩张。开胸肺活检显示为类脂性肺炎。由于没有滴鼻用油史,诊断为特发性类脂性肺炎。并对相关文献进行了综述。

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